DK174615B1 - Fremgangsmåde til fremstilling af 5-aminosalicylsyre - Google Patents
Fremgangsmåde til fremstilling af 5-aminosalicylsyre Download PDFInfo
- Publication number
- DK174615B1 DK174615B1 DK198703507A DK350787A DK174615B1 DK 174615 B1 DK174615 B1 DK 174615B1 DK 198703507 A DK198703507 A DK 198703507A DK 350787 A DK350787 A DK 350787A DK 174615 B1 DK174615 B1 DK 174615B1
- Authority
- DK
- Denmark
- Prior art keywords
- acid
- salicylic acid
- reaction
- sulphanilic
- sodium
- Prior art date
Links
- KBOPZPXVLCULAV-UHFFFAOYSA-N mesalamine Chemical compound NC1=CC=C(O)C(C(O)=O)=C1 KBOPZPXVLCULAV-UHFFFAOYSA-N 0.000 title claims description 26
- 229960004963 mesalazine Drugs 0.000 title claims description 26
- 238000000034 method Methods 0.000 title claims description 20
- 238000002360 preparation method Methods 0.000 title claims description 5
- YGSDEFSMJLZEOE-UHFFFAOYSA-N salicylic acid Chemical compound OC(=O)C1=CC=CC=C1O YGSDEFSMJLZEOE-UHFFFAOYSA-N 0.000 claims description 20
- HVBSAKJJOYLTQU-UHFFFAOYSA-N 4-aminobenzenesulfonic acid Chemical compound NC1=CC=C(S(O)(=O)=O)C=C1 HVBSAKJJOYLTQU-UHFFFAOYSA-N 0.000 claims description 15
- 229950000244 sulfanilic acid Drugs 0.000 claims description 15
- FJKROLUGYXJWQN-UHFFFAOYSA-N papa-hydroxy-benzoic acid Natural products OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 claims description 10
- 229960004889 salicylic acid Drugs 0.000 claims description 10
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 8
- 239000003054 catalyst Substances 0.000 claims description 7
- MXCDRFGKHNFKIP-UHFFFAOYSA-N 2-hydroxy-5-[(4-sulfophenyl)diazenyl]benzoic acid Chemical compound C1=C(O)C(C(=O)O)=CC(N=NC=2C=CC(=CC=2)S(O)(=O)=O)=C1 MXCDRFGKHNFKIP-UHFFFAOYSA-N 0.000 claims description 5
- 239000012452 mother liquor Substances 0.000 claims description 5
- 159000000000 sodium salts Chemical class 0.000 claims description 5
- 239000000126 substance Substances 0.000 claims description 5
- 238000000354 decomposition reaction Methods 0.000 claims description 4
- 230000020477 pH reduction Effects 0.000 claims description 4
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 claims description 4
- 238000005984 hydrogenation reaction Methods 0.000 claims description 3
- 229910052763 palladium Inorganic materials 0.000 claims description 3
- 239000002244 precipitate Substances 0.000 claims description 3
- 229910052697 platinum Inorganic materials 0.000 claims description 2
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 claims 2
- UEUIKXVPXLWUDU-UHFFFAOYSA-O 4-sulfobenzenediazonium Chemical compound OS(=O)(=O)C1=CC=C([N+]#N)C=C1 UEUIKXVPXLWUDU-UHFFFAOYSA-O 0.000 claims 1
- 229910052723 transition metal Inorganic materials 0.000 claims 1
- 150000003624 transition metals Chemical class 0.000 claims 1
- 238000006243 chemical reaction Methods 0.000 description 11
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 10
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 9
- 239000012954 diazonium Substances 0.000 description 9
- 150000001989 diazonium salts Chemical class 0.000 description 8
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
- 239000000047 product Substances 0.000 description 6
- 238000001816 cooling Methods 0.000 description 5
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 4
- 238000007792 addition Methods 0.000 description 4
- 238000003776 cleavage reaction Methods 0.000 description 4
- 229910001873 dinitrogen Inorganic materials 0.000 description 4
- VWDWKYIASSYTQR-UHFFFAOYSA-N sodium nitrate Chemical compound [Na+].[O-][N+]([O-])=O VWDWKYIASSYTQR-UHFFFAOYSA-N 0.000 description 4
- LPXPTNMVRIOKMN-UHFFFAOYSA-M sodium nitrite Chemical compound [Na+].[O-]N=O LPXPTNMVRIOKMN-UHFFFAOYSA-M 0.000 description 4
- KSVSZLXDULFGDQ-UHFFFAOYSA-M sodium;4-aminobenzenesulfonate Chemical compound [Na+].NC1=CC=C(S([O-])(=O)=O)C=C1 KSVSZLXDULFGDQ-UHFFFAOYSA-M 0.000 description 4
- 239000012467 final product Substances 0.000 description 3
- 239000011541 reaction mixture Substances 0.000 description 3
- 230000007017 scission Effects 0.000 description 3
- JVBXVOWTABLYPX-UHFFFAOYSA-L sodium dithionite Chemical compound [Na+].[Na+].[O-]S(=O)S([O-])=O JVBXVOWTABLYPX-UHFFFAOYSA-L 0.000 description 3
- 238000003756 stirring Methods 0.000 description 3
- PLIKAWJENQZMHA-UHFFFAOYSA-N 4-aminophenol Chemical compound NC1=CC=C(O)C=C1 PLIKAWJENQZMHA-UHFFFAOYSA-N 0.000 description 2
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 2
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 238000004811 liquid chromatography Methods 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 239000004317 sodium nitrate Substances 0.000 description 2
- 235000010344 sodium nitrate Nutrition 0.000 description 2
- 235000010288 sodium nitrite Nutrition 0.000 description 2
- 238000005406 washing Methods 0.000 description 2
- AFPHTEQTJZKQAQ-UHFFFAOYSA-N 3-nitrobenzoic acid Chemical compound OC(=O)C1=CC=CC([N+]([O-])=O)=C1 AFPHTEQTJZKQAQ-UHFFFAOYSA-N 0.000 description 1
- AVXURJPOCDRRFD-UHFFFAOYSA-N Hydroxylamine Chemical compound ON AVXURJPOCDRRFD-UHFFFAOYSA-N 0.000 description 1
- 238000006612 Kolbe reaction Methods 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 238000005576 amination reaction Methods 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 238000007664 blowing Methods 0.000 description 1
- 239000001569 carbon dioxide Substances 0.000 description 1
- 229910002092 carbon dioxide Inorganic materials 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 230000007812 deficiency Effects 0.000 description 1
- 238000006193 diazotization reaction Methods 0.000 description 1
- GRWZHXKQBITJKP-UHFFFAOYSA-L dithionite(2-) Chemical compound [O-]S(=O)S([O-])=O GRWZHXKQBITJKP-UHFFFAOYSA-L 0.000 description 1
- 229940079593 drug Drugs 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 239000000706 filtrate Substances 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 239000002920 hazardous waste Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- -1 hydrogen ions Chemical class 0.000 description 1
- 238000009776 industrial production Methods 0.000 description 1
- 230000000802 nitrating effect Effects 0.000 description 1
- 239000000825 pharmaceutical preparation Substances 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 239000002002 slurry Substances 0.000 description 1
- 150000003464 sulfur compounds Chemical class 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 230000008719 thickening Effects 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C227/00—Preparation of compounds containing amino and carboxyl groups bound to the same carbon skeleton
- C07C227/04—Formation of amino groups in compounds containing carboxyl groups
- C07C227/06—Formation of amino groups in compounds containing carboxyl groups by addition or substitution reactions, without increasing the number of carbon atoms in the carbon skeleton of the acid
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C227/00—Preparation of compounds containing amino and carboxyl groups bound to the same carbon skeleton
- C07C227/14—Preparation of compounds containing amino and carboxyl groups bound to the same carbon skeleton from compounds containing already amino and carboxyl groups or derivatives thereof
- C07C227/18—Preparation of compounds containing amino and carboxyl groups bound to the same carbon skeleton from compounds containing already amino and carboxyl groups or derivatives thereof by reactions involving amino or carboxyl groups, e.g. hydrolysis of esters or amides, by formation of halides, salts or esters
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| SE8603007 | 1986-07-07 | ||
| SE8603007A SE462095B (sv) | 1986-07-07 | 1986-07-07 | Saett att framstaella 5-aminosalicylsyra |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| DK350787D0 DK350787D0 (da) | 1987-07-07 |
| DK350787A DK350787A (da) | 1988-01-08 |
| DK174615B1 true DK174615B1 (da) | 2003-07-21 |
Family
ID=20365049
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DK198703507A DK174615B1 (da) | 1986-07-07 | 1987-07-07 | Fremgangsmåde til fremstilling af 5-aminosalicylsyre |
Country Status (15)
| Country | Link |
|---|---|
| US (1) | US4788331A (es) |
| EP (1) | EP0253788B1 (es) |
| JP (1) | JPH0774186B2 (es) |
| AR (1) | AR245098A1 (es) |
| AU (1) | AU601749B2 (es) |
| CA (1) | CA1287643C (es) |
| DE (1) | DE3776440D1 (es) |
| DK (1) | DK174615B1 (es) |
| FI (1) | FI88711C (es) |
| IL (1) | IL82977A (es) |
| IN (1) | IN167686B (es) |
| MX (1) | MX172546B (es) |
| NO (1) | NO167976C (es) |
| NZ (1) | NZ220983A (es) |
| SE (1) | SE462095B (es) |
Families Citing this family (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE4020056A1 (de) * | 1990-06-23 | 1992-01-02 | Bayer Ag | Verfahren zur herstellung sehr reiner 5-aminosalicylsaeure |
| DE10029410A1 (de) | 2000-06-15 | 2002-01-03 | Bfgoodrich Diamalt Gmbh | Verfahren zur Herstellung von 5-Aminosalicylsäure |
| CA2495537C (en) | 2000-08-29 | 2010-03-30 | Nobex Corporation | Immunoregulatory compounds and derivatives and methods of treating diseases therewith |
| US8048924B2 (en) | 2001-08-29 | 2011-11-01 | Biocon Limited | Methods and compositions employing 4-aminophenylacetic acid compounds |
| DK1773767T3 (en) | 2004-07-07 | 2016-03-21 | Biocon Ltd | Synthesis of azo bound in immune regulatory relations |
| US20090036414A1 (en) * | 2007-08-02 | 2009-02-05 | Mutual Pharmaceutical Company, Inc. | Mesalamine Formulations |
| KR100852962B1 (ko) * | 2007-11-12 | 2008-08-20 | 주식회사 뉴로테크 | 2-하이드록시-5-페닐알킬아미노벤조산 유도체 및 이의 염의제조방법 |
| JP5581927B2 (ja) * | 2010-09-14 | 2014-09-03 | オリヱント化学工業株式会社 | ４−アミノ−ｍ−クレゾールの製造方法 |
| CN111548283A (zh) * | 2020-03-22 | 2020-08-18 | 浙江华贝药业有限责任公司 | 5-氨基水杨酸一锅催化合成方法 |
| CN117088784A (zh) * | 2023-10-18 | 2023-11-21 | 广州市桐晖药业有限公司 | 一种美沙拉嗪的合成方法 |
Family Cites Families (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US1542265A (en) * | 1922-10-20 | 1925-06-16 | James F Norris | Process of making aminosalicylic acid |
| US1727468A (en) * | 1927-02-09 | 1929-09-10 | Gen Aniline Works Inc | Azo dyestuff containing chromium |
| US2658673A (en) * | 1945-02-13 | 1953-11-10 | Bell Telephone Labor Inc | Ballistic computer having range extending adjustable scale factor means |
| US3063980A (en) * | 1957-07-09 | 1962-11-13 | Gen Aniline & Film Corp | Process for reducing aromatic nitrogen compounds |
| DE2806950C2 (de) * | 1978-02-18 | 1982-05-19 | Bayer Ag, 5090 Leverkusen | Eisenkomplexazofarbstoffe und deren Verwendung |
| SU1159919A1 (ru) * | 1983-05-23 | 1985-06-07 | Предприятие П/Я А-7850 | Способ получени 5-аминосалициловой кислоты |
| DE3638364A1 (de) * | 1986-11-11 | 1988-05-19 | Bayer Ag | Verfahren zur herstellung von 5-aminosalicylsaeure |
-
1986
- 1986-07-07 SE SE8603007A patent/SE462095B/sv not_active IP Right Cessation
-
1987
- 1987-06-17 DE DE8787850198T patent/DE3776440D1/de not_active Expired - Lifetime
- 1987-06-17 EP EP87850198A patent/EP0253788B1/en not_active Expired - Lifetime
- 1987-06-24 IN IN536/DEL/87A patent/IN167686B/en unknown
- 1987-06-24 IL IL82977A patent/IL82977A/xx not_active IP Right Cessation
- 1987-07-02 AR AR87308042A patent/AR245098A1/es active
- 1987-07-03 JP JP62166764A patent/JPH0774186B2/ja not_active Expired - Lifetime
- 1987-07-03 CA CA000541202A patent/CA1287643C/en not_active Expired - Lifetime
- 1987-07-06 AU AU75258/87A patent/AU601749B2/en not_active Ceased
- 1987-07-06 NO NO872809A patent/NO167976C/no not_active IP Right Cessation
- 1987-07-06 FI FI872977A patent/FI88711C/fi not_active IP Right Cessation
- 1987-07-06 MX MX007219A patent/MX172546B/es unknown
- 1987-07-07 NZ NZ220983A patent/NZ220983A/xx unknown
- 1987-07-07 US US07/079,591 patent/US4788331A/en not_active Expired - Lifetime
- 1987-07-07 DK DK198703507A patent/DK174615B1/da not_active IP Right Cessation
Also Published As
| Publication number | Publication date |
|---|---|
| FI88711C (fi) | 1993-06-28 |
| NO167976C (no) | 1992-01-02 |
| AR245098A1 (es) | 1993-12-30 |
| SE462095B (sv) | 1990-05-07 |
| SE8603007D0 (sv) | 1986-07-07 |
| NO167976B (no) | 1991-09-23 |
| NO872809L (no) | 1988-01-08 |
| JPS6339843A (ja) | 1988-02-20 |
| IN167686B (es) | 1990-12-08 |
| FI872977A0 (fi) | 1987-07-06 |
| FI88711B (fi) | 1993-03-15 |
| NO872809D0 (no) | 1987-07-06 |
| JPH0774186B2 (ja) | 1995-08-09 |
| AU601749B2 (en) | 1990-09-20 |
| FI872977A (fi) | 1988-01-08 |
| AU7525887A (en) | 1988-01-14 |
| MX172546B (es) | 1994-01-03 |
| EP0253788A2 (en) | 1988-01-20 |
| DK350787A (da) | 1988-01-08 |
| DE3776440D1 (de) | 1992-03-12 |
| EP0253788B1 (en) | 1992-01-29 |
| EP0253788A3 (en) | 1989-03-29 |
| SE8603007L (sv) | 1988-01-08 |
| NZ220983A (en) | 1989-10-27 |
| US4788331A (en) | 1988-11-29 |
| DK350787D0 (da) | 1987-07-07 |
| IL82977A0 (en) | 1987-12-20 |
| CA1287643C (en) | 1991-08-13 |
| IL82977A (en) | 1990-12-23 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| DK174615B1 (da) | Fremgangsmåde til fremstilling af 5-aminosalicylsyre | |
| NO149176B (no) | Fremgangsmaate for fremstilling av n-fosfonometyl-glycin | |
| JPS59144734A (ja) | 親水性フエノ−ルエステル誘導体の合成法 | |
| KR100271775B1 (ko) | 2-알킬-6-메틸-n-(1'-메톡시-2'-프로필)-아날린의 제조방법 및 이들의 클로르아세트아닐리드의 제조방법 | |
| KR20070039948A (ko) | 2-아미노-5-요오도 안식향산의 제조 방법 | |
| Varkey et al. | Activation of dimethyl sulfoxide by electrophiles and use of the reactive intermediates in the preparation of iminosulfuranes | |
| JP2754243B2 (ja) | ４‐クロロ‐２，５‐ジメトキシアニリンの製造方法 | |
| EP0415595A1 (en) | Fluorobenzene derivatives | |
| KR860001366B1 (ko) | N-포르밀-l-아스파르트산 무수물의 제조방법 | |
| JPH05286889A (ja) | アリール酢酸及びそれらのアルカリ金属塩の製造方法 | |
| JPS62123168A (ja) | マレイミド類の製造方法 | |
| US5523472A (en) | Process for the preparation of 5-fluoroanthranilic acid | |
| EP0092487B1 (en) | Process for the preparation of 3-carboxy-1,4-dimethylpyrrol-2-acetic acid | |
| EP0105664B1 (en) | Process for the preparation of 3-carboxy-1-methylpyrrol-2-acetic-acid and alkali metal salts thereof | |
| US5688969A (en) | Process for the preparation of thiophene-2-5-dicarboxylic acid and the dichloride thereof | |
| KR100549354B1 (ko) | 케토산의정제방법 | |
| EP0089332B1 (en) | Preparation or ortho-methyl anilines from ortho-amino benzyl sulfoxides | |
| JPS6270350A (ja) | ベンゾフエノン誘導体の製造法 | |
| RU2268261C2 (ru) | Способ получения динатриевой соли фенилен-бис-бензимидазол-тетрасульфоновой кислоты | |
| US5245058A (en) | Preparation of 1-nitroanthraquinone-2-carboxylic acids | |
| KR910009235B1 (ko) | 3-메톡시-6-아닐리노 톨루엔의 제조방법 | |
| GB1575860A (en) | Process for the manufacture of m-aminophenols | |
| HU214022B (en) | Process for producing high-purity 4-nitrobenzoic acid | |
| JPH01221356A (ja) | ３‐アミノ‐４‐トリフルオロメチル安息香酸およびその製造方法 | |
| JPH0273035A (ja) | メトキシ酢酸の製造法 |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PUP | Patent expired |